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. 2004 Jun 15;91(2):297–304. doi: 10.1038/sj.bjc.6601946

Cytotoxic effect of a new 1,3,4-thiadiazolium mesoionic compound (MI-D) on cell lines of human melanoma

A Senff-Ribeiro 1, A Echevarria 2, E F Silva 2, C R C Franco 3, S S Veiga 3, M B M Oliveira 1,*
PMCID: PMC2409799  PMID: 15199390

Abstract

The structural characteristics of mesoionic compounds, which contain distinct regions of positive and negative charges associated with a poly-heteroatomic system, enable them to cross cellular membranes and interact strongly with biomolecules. Potential biological applications have been described for mesoionic compounds. 1,3,4-Thiadiazolium mesoionic compound (MI-D), a new mesoionic compound, has been demonstrated to be extremely cytotoxic to B16-F10 murine melanoma cells when compared to fotemustine and dacarbazine, drugs of reference in melanoma treatment protocols, describing inhibition of tumours grown in vitro and in vivo. We now evaluate the effects of mesoionic compound MI-D on different human melanoma cell lines. The drug decreased the viability and proliferation of MEL-85, SK-MEL, A2058 and MEWO cell lines in vitro, showing a considerable cytotoxic activity on these human cells. Adhesion of MEL-85 cells was evaluated in the presence of the drug using different extracellular matrix (ECM) constituents. MI-D decreased MEL-85 adhesion to laminin, fibronectin and matrigel. The morphology and actin cytoskeleton organisation of MEL-85 cells were also modified on MI-D treatment. These results on human melanoma cell lines indicate that MI-D is a very encouraging drug against melanoma, a tumour that is extremely resistant to chemotherapy.

Keywords: mesoionic compounds, MI-D, antimelanoma activity, human melanoma cell lines

Compounds of the mesoionic class have interesting structural features provided by their betaine-like character. They consist of a five-membered heterocyclic ring associated with a sextet of p and π electrons, supporting a partial positive charge in the heterocyclic ring, which is counterbalanced by a formal negative charge on the atom of the α-side chain (Ollis and Ramsden, 1976; Newton and Ramsden, 1982; Cheung et al, 1992). The association of these characteristics suggests a high probability of strong interactions with biomolecules such as DNA and/or proteins. Although mesoionic compounds are internally charged, they are neutral overall, and can therefore cross biological membranes in vivo (Kier and Roche, 1967).

All the different classes of mesoionic compounds (sydnones, sydnonimines, isosydnones and 1,3,4-thiadiazoles) have received considerable attention and have been extensively studied because of their unique structures, reaction behaviour, biological activities and possible pharmaceutical use (Moustafa and Eisa, 1991; Corell et al, 1994; Rehse et al, 1995; Satyanarayana and Rao, 1995). These include anti-inflammatory, analgesic, antibacterial, antifungal and antitumour activities (Badachikar et al, 1986; Shinzato et al, 1989; Moustafa and Eisa, 1991; Grynberg et al, 1992; Montanari et al, 1992; Satyanarayana and Rao, 1995; Grynberg et al, 1997; Senff-Ribeiro et al, 2003, 2004). Potent antiplatelet, fibrinolytic, thrombolytic and broncholytic effects (Corell et al, 1994; Kankaanranta et al, 1996), and effects on the cardiovascular system (Majid et al, 1980; Rudolph and Derschinger, 1991; Rehse and Konig, 1995; Rehse et al, 1995) have also been described for mesoionic compounds. Some effects described for these compounds are intimately related to the presence of specific substituent groups on the ring (Corell et al, 1994; Satyanarayana and Rao, 1995; Kankaanranta et al, 1996; Grynberg et al, 1997), or to the ability to release nitric oxide from their molecular structures (Hogg et al, 1992).

A new mesoionic compound, 4-phenyl-5-(4-nitrocinnamoyl)-1,3,4-thiadiazolium-2-phenylamine chloride (MI-D) was synthesised by Grynberg et al (1997) (Figure 1), for which it was shown the enhancement of the survival of Ehrlich carcinoma and Sarcoma-180 tumour-bearing mice, preventing tumour growth, with no significant concomitant alterations in the haematological parameters of tested animals, at a dose of 25 mg kg−1 (57 μmol kg−1).

Figure 1.

Figure 1

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Chemical structure of 4-phenyl-5-(4-nitrocinnamoyl)-1,3,4-thiadiazolium-2-phenylamine chloride (MI-D).

MI-D was shown to be able to inhibit the respiratory chain between complexes II and III, collapse the transmembrane potential, and stimulate ATPase activity in intact mitochondria (Cadena et al, 1998). Alterations were also reported in membrane permeability and fluidity, which are related to its effect on the energy-linked functions of mitochondria (Cadena et al, 2002).

Recent studies in our laboratory evaluating a series of 1,3,4-thiadiazolium mesoionics showed that MI-D, which has an NO2 substituent on the cinnamoyl ring, was the most effective against the melanoma murine model B16-F10 (Senff-Ribeiro et al, 2004). Compared with two other antineoplastic agents (fotemustine and dacarbazine), it was effective against the murine model both in vitro and in vivo, under the same experimental conditions and with the same molar concentrations (Senff-Ribeiro et al, 2003).

Although antitumour effects against Ehrlich and Sarcoma-180 tumour models, and even against the aggressive melanoma murine model B16-F10, have already been demonstrated for MI-D (Grynberg et al, 1997; Senff-Ribeiro et al, 2003, 2004), it has not been tested against human melanoma cell lines.

We now study the effects of MI-D on four established human melanoma cell lines: MEL-85, SK-MEL, A2058 and MEWO. The in vitro viabilities and proliferations of these cell lines in the presence of MI-D were evaluated. In order to obtain further insights concerning MI-D's anti-melanoma activity, cell features of adhesion, morphology and actin cytoskeleton organisation, which are deeply related to the development and establishment of tumours, were also subjects studied using the MEL-85 cell line.

MATERIALS AND METHODS

Materials

MI-D (4-phenyl-5-(4-nitro-cinnamoyl)-1,3,4-thiadiazolium-2-phenylamine chloride) was synthesised in the Department of Chemistry of the Rural Federal University of Rio de Janeiro, Brazil, as described elsewhere (Grynberg et al, 1997). Its structure was confirmed by 1H- and 13C-NMR spectroscopy and mass spectrometry. Dulbecco's modified Eagle's medium (DMEM), RPMI1640 medium and fetal bovine serum (FBS) were obtained from Cultilab (Campinas, Brazil); penicillin and gentamycin were both purchased from GIBCO (Bethesda, USA). Paraformaldehyde (20%, aqueous solution) was from EMS (Electron Microscopy Sciences, Washington, USA). Phalloidin labelled with FITC was from Molecular Probes (Eugene, USA) and the aqueous mounting medium, Fluormount-G® from EMS (Washington, USA). Trypan blue, MTT, crystal violet and glycine were obtained from Sigma Aldrich (St Louis, USA). DMSO was from Merck. All other reagents were commercial products of the highest available purity grade.

Drug solutions

MI-D was dissolved in dimethylsulphoxide (DMSO) for its experimental use. In order to minimise solvent interference, several stock solutions of MI-D were prepared so that at the desired final concentrations of MI-D in the assays, the amounts of DMSO were identical and equal to 0.12%.

Cell lines and culture conditions

Human melanoma cell lines used in this study were kindly provided by the Ludwig Institute for Cancer Research (São Paulo, Brazil). Cells were maintained in liquid nitrogen with a low number of passages. After thawing, the cells were grown in monolayer cultures in the appropriate media containing penicillin (100 U ml−1) and gentamicin (50 μg ml−1). MEL-85 and MEWO cells were cultured in RPMI containing 10% FBS, SK-MEL cells in RPMI containing 15% FBS and A2058 cells in DMEM containing 10% FBS. The cultures were kept at 37°C under a humidified atmosphere plus 5% CO2. Release of cells was performed by a treatment for a few minutes with a 2 mM solution of ethylenediaminetetraacetic acid (EDTA) in phosphate-buffered saline (PBS). After being counted, cells were then resuspended in an adequate volume of the respective medium supplemented with FBS and again plated in the presence or absence of MI-D.

Cell viability assay

Viability assays were carried out on 24-well plates (TPP, Trasadingen, Switzerland). Human melanoma cells (5 × 105 cells well−1) were plated and allowed to adhere and grown for 20 h before incubation with the drug. MI-D was added in varying concentrations up to 75 μM. At each determined interval (24 and 48 h), supernatants and cells were harvested, centrifuged, washed with PBS and the viability was measured by the Trypan blue-exclusion assay (Phillips, 1973). Briefly, Trypan blue (0.4% in PBS, pH 7.4) was added to the cell suspension and the number of viable (unstained) and nonviable (stained) cells was counted using a Neubauer Chamber. For control experiments, the appropriate medium contained adequate amounts of vehicle (0.12% of DMSO). Cell viability of controls was normalised to 100%.

Cell proliferation assay

Human melanoma cells (6 × 103 cells well−1) were grown for 16 h on 96-well plates (TPP) containing an appropriate medium supplemented with an adequate amount of FBS. The medium was then replaced by a serum-free one. After 24 h, this was replaced with the respective medium containing the usual concentrations of FBS plus MI-D, at different concentrations (2.5–25 μM) in quadruplicate. Controls consisted of the respective medium alone or in the presence of 0.12% DMSO, which was the MI-D solvent. After 24, 48 and 72 h the number of cells in each well was determined using the MTT method (Mosmann, 1983). MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide] was dissolved in Hanks’ balanced saline solution (HBSS) at 5 mg ml−1. At the above intervals, 20 μl of the MTT solution were added to each well and the plates were incubated at 37°C for 3 h. The MTT solution was removed and DMSO was added and mixed thoroughly to dissolve the dark-blue crystals. The plates were then read using a Microelisa Reader (Bio-Rad, Madison, USA) at 550 nm for sample and 655 nm for reference. Results are expressed as the cell number, which was determined using a standard curve of cells against absorbance.

Cell adhesion assay

Native fibronectin was purified from fresh human plasma according to the procedure of Engvall and Ruoslahti (1977). Laminin and matrigel, a reconstituted basement membrane, were purified from a Engelbreth–Holm–Swarm (EHS) tumour as described by Paulsson et al (1987) and Kleinman et al (1986), respectively. The presence and purity of proteins were assessed by both an electrophoretic analysis on sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS–PAGE) and Western blot. Adhesion assays were performed as described by Saiki et al (1989) with some modifications. Briefly, MEL-85 cells (4 × 104) with or without MI-D (0.5, 1.0, 2.5 and 5.0 μM) were added to microculture wells (96-well plates, TPP) precoated with fibronectin, laminin or matrigel (10 μg ml−1) and blocked with bovine serum albumin (BSA) 1%. The cultures were incubated at 37°C for 2 h. The wells were washed twice with warm PBS to remove unattached cells, and then the attached cells were fixed with methanol and stained with 0.8% crystal violet dissolved in 20% ethanol. After extensive washing with PBS, the dye was eluted with 50% ethanol in 0.05 M sodium citrate and the absorbance was measured at 550 nm using a MicroElisa Reader (BioRad). At the end of the experiment, the plates were photographed (Leica-MPS30) using an inverted microscope (Leica-DMIL). The control contained the same amount of DMSO as the tested wells (0.12% of DMSO) and its cellular adhesion was normalised to 100%.

Cell morphology analysis

MEL-85 cells were cultured on glass coverslides for 16 h at 37°C under a humidified atmosphere plus 5% CO2. Cells were treated with 25 and 50 μM MI-D for 2 h. After treatment, they were washed twice with PBS and fixed with 2% paraformaldehyde in PBS for 30 min at 4°C. For the control, the appropriate medium contained adequate amounts of vehicle (0.12% of DMSO). Coverslides were stained by Giemsa and studied by bright-field microscopy (Olympus BX40). Images were acquired (× 400) in grayscale using a software Image-Plus 4.0 version (Media Cybernetics, Silver Spring, USA). A morphometric analysis was performed using an ImageTool software 3.00 version (University of Texas Health Science Center in San Antonio, USA). Cell features, such as area, elongation and roundness of about 400 cells were analysed. For analysis, the area of the object, measured as the number of pixels in the polygon was converted to percent. Elongation was measured as the ratio of the length of the major axis to the length of the minor axis. The result was a value of between 0 and 1 that was converted to % for analysis to obtain an analytical value. Roundness was computed as: (4π × area)/perimeter2. The result gave a value of between 0 and 1 that was converted to % for analysis.

Immunofluorescence microscopy

MEL-85 cells (5 × 104) were plated on glass coverslides (13 mm diameter), which were prepared for confocal immunofluorescence microscopy. After 16 h, MEL-85 cells were incubated with 50 μM MI-D for 2 h at 37°C under a humidified atmosphere plus 5% CO2. In the control, the appropriate medium contained adequate amounts of vehicle (0.12% of DMSO). Cells were washed twice with PBS and fixed with 2% paraformaldehyde in PBS for 30 min at 4°C. Cells on coverslides were incubated with 0.1 M glycine for 3 min, washed with PBS and then blocked with PBS containing 1% BSA for 30 min at room temperature (25°C). After washing thrice with PBS, coverslides were incubated with phalloidine conjugated with fluorescein isothiocyanate (FITC) (Molecular Probes) diluted in PBS (1 : 200) for 20 min. After washing with PBS (10 ×) and once in water, slides were mounted with Fluormont-G®. Cells were observed using a confocal fluorescence microscope (Confocal Radiance 2100, Bio-Rad) coupled to a Nikon Eclipse 800 with plan apochromatic objectives (Science and Technologies Group Instruments Division, Melville, USA). Images were acquired (× 600) using Radiance 2100 (Bio-Rad).

Statistical analysis

Statistical analysis of data were carried out using analysis of variance (ANOVA) and the Tukey test for average comparison. Mean±s.d. values were used. Significance was defined as P<0.05.

RESULTS

Effect of MI-D on cell viability

Figure 2 shows the effect of the mesoionic compound on the viability of human melanoma cell lines evaluated 24 and 48 h after treatment with different concentrations of MI-D (2.5–75 μM). Time- and dose-dependent effects were shown by MI-D on the four cell lines studied.

Figure 2.

Figure 2

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Effects of MI-D on the viability of different human melanoma cell lines. (A) Effects of MI-D on MEL-85 cells. (B) Effects of MI-D on SK-MEL cells. (C) Effects of MI-D on A2058 cells. (D) Effects of MI-D on MEWO cells. The viability of melanoma cells was measured at indicated intervals and concentrations of MI-D using the trypan blue-exclusion assay (n=4). Values given are the mean±s.d. *P<0.001.

The viability of MEL-85 cells was reduced to 56% after a 24 h treatment with 10 μM MI-D (Figure 2A). At this time of incubation, 75 μM MI-D diminished the viability by ∼82%. When a treatment of 48 h was used, the maximum cytotoxic effect (100%) was reached starting from 50 μM. A measure of 5 μM MI-D reduced the number of viable cells to 27% after 48 h incubation.

SK-MEL cells also had their viability diminished by MI-D treatment (Figure 2B). After 24 h, 25 μM MI-D reduced the viability to ∼30% and at 50 μM to 17%. When the concentration was raised to 75 μM, there were no viable cells after 24 h incubation. A volume of 10 μM MI-D reduced the viability to 30% after 48 h. At this time, there was more than 90% of cell death using 50 μM MI-D.

The viability of A2058 cells was decreased to ∼30% when the concentration of MI-D was 10 μM and the incubation time was 24 h (Figure 2C). At this time, the concentrations of 25 and 50 μM reduced the number of viable cells to 12 and 7%, respectively. When a 48 h incubation was assayed, 10 μM MI-D reduced the viability to 20% and 25 μM almost gave a maximum cytotoxic effect (97%). At this time, all A2058 cells were dead when the concentration of MI-D was 50 μM.

MEWO cells were also very sensitive to the toxic effects of MI-D (Figure 2D). After 24 h, MI-D at 10 and 25 μM concentrations, diminished the viability to 23 and 8%, respectively. Increasing the drug concentration to 75 μM resulted in only ∼1% of viable cells after 24 h. When a 48 h treatment was performed, 10 μM MI-D reduced the number of viable cells to 13% while 50 μM gave rise to ∼100% cell death.

Effect of MI-D on cell growth

Evaluation of the effect of MI-D on the growth of human melanoma cell lines was performed using a growth–time kinetic study of up to 72 h (Figure 3). Proliferation of all melanoma cell lines was greatly inhibited by MI-D, even when subcytotoxic concentrations (1–2.5 μM) were tested.

Figure 3.

Figure 3

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Effects of MI-D on the proliferation of human melanoma cell lines. (A) Effects of MI-D on MEL-85 cells. (B) Effects of MI-D on SK-MEL cells. (C) Effects of MI-D on A2058 cells. (D) Effects of MI-D on MEWO cells. The proliferation rates were measured using the MTT method at the times indicated and at subcytotoxic (2.5 μM) and cytotoxic (5–25 μM) concentrations (n=3). Values given are the mean±s.d. *P<0.01 **P<0.001.

MEL-85 cells (Figure 3A) treated with 5 μM MI-D gave a 50% reduction of cell growth during the 72 h experiment. At a concentration of 10 μM, the proliferation of MEL-85 cells was completely inhibited.

No growth of SK-MEL cells (Figure 3B) was observed when 5 μM MI-D was used. After 24 h, 1 and 2.5 μM MI-D reduced the number of cells to ∼65 and ∼55%, respectively.

A2058 cells (Figure 3C) had their growth reduced to 55–61% when the concentration was 2.5 μM. When MI-D was used at 5 μM, there was no increase in cell number up to 48 h. However, at 72 h there was a recovery and the number of cells increased, being 46% of the control.

The proliferation of MEWO cells was inhibited by MI-D (Figure 3D). At a low MI-D dose (2.5 μM) a decrease of cell number of a quarter after 48 and 72 h was observed. The concentration of 5 μM allowed cell growth up to 24 h, but after there was no increase in cell number up to 72 h. In all, 10 μM MI-D did not allow MEWO growth. It must be pointed out that all cell lines, when exposed to MI-D at 10 μM or more, did not grow and extensive cell death was observed, confirming the previous data appearing in Figure 2.

Effect of MI-D on MEL-85 adhesion to laminin, fibronectin and matrigel

Figure 4 shows the effects of MI-D on MEL-85 adhesion to extracellular matrix (ECM) constituents, such as laminin, fibronectin and matrigel. Although there were apparent decreases on cell adhesion when 0.5 and 1 μM of MI-D were used, the values were not statistically different from those of the controls. Higher concentrations of MI-D significantly inhibited MEL-85 adhesion to ECM molecules in a concentration-dependent manner. Adhesion to laminin and fibronectin was decreased to 70 and 55% by 2.5 and 5 μM of MI-D, respectively, after 2 h exposure (Figures 4A and B). At 5 μM, MI-D diminished MEL-85 adhesion to laminin to ∼65% (Figure 4A) and to fibronectin and matrigel to 34 and 71%, respectively (Figure 4B and C). The micrographs of the adhesion on fibronectin (Figure 4D) show that MI-D not only reduced the number of cells adhering to fibronectin, but also altered the morphology of MEL-85 cells, which shrinked and became round. These changes were also observed when cells were assayed for their adhesion on laminin and matrigel (data not shown).

Figure 4.

Figure 4

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Effects of MI-D on the adhesion of MEL-85 human melanoma cell to ECM constituents. (A) MEL-85 adhesion to laminin. (B) MEL-85 adhesion to fibronectin. (C) MEL-85 adhesion to matrigel. (D) Micrographs of MEL-85 cells adhered to fibronectin. (1) Control cells, (2) cells treated with 2.5 μM MI-D, (3) cells treated with 5 μM MI-D. MEL-85 cells (4 × 104) were added to microculture wells precoated with ECM constituents in the presence of indicated concentrations of MI-D. After a 2 h incubation, nonadherent cells were washed and adherent cells were fixed and stained with 0.8% (p v−1) crystal violet containing 20% methanol. After extensive washing, the stained cells were lysed with 50% ethanol in 0.05 M sodium citrate and the absorbance was measured at 550 nm. **P<0.01 and ***P<0.001.

Effect of MI-D on MEL-85 morphology

Figure 5 shows micrographs of MEL-85 cells stained by Giemsa. It can be observed with treated cells (Figure 5B and C) that the presence of MI-D gave rise to a disruption of the interactions between cells and substratum. MI-D treated cells are not so spread out as control cells (Figure 5A). The results clearly demonstrate significant changes in cell shape, with cells becoming round when compared to those of the control, as was also observed in adhesion assays. The treatment with 25 μM MI-D gave rise to shrinkage of some cells, presenting protrusions of the plasma membrane, which were pinched off to form membrane-enclosed similar apoptotic bodies probably with cytoplasmic and nuclear contents. Intense vacuolisation of cytoplasm was observed with treated cells. The concentration of 50 μM affected the morphology of almost all of the cells. Condensed chromatin masses with intense eosinophilia and pyknotic nuclei were also observed with treated cells. Morphometric analysis permitted quantification of morphological changes and showed a reduction of 35% in the area of cells treated with 50 μM MI-D. This concentration reduced cell elongation to 56% and increased cell roundness by 112%.

Figure 5.

Figure 5

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Effects of MI-D on the morphology of MEL-85 cells. (A) Micrographs of control cells. (B) Micrographs of MEL-85 cells treated with 25 μM MI-D. (C) Micrographs of MEL-85 cells treated with 50 μM MI-D. MEL-85 cells were treated for 2 h, fixed and stained with Giemsa. Samples were observed using a bright-field microscope (Olympus BX40). Closed arrows point to cell shrinkage. Closed arrowheads show vacuolisation of cytoplasm. Open arrows indicate chromatin condensation. Open arrowheads indicate bleb formation in cell membranes (× 400).

Effect of MI-D on MEL-85 cytoskeleton organisation

In order to evaluate if the changes on cell shape were due to alterations on the actin organisation, an experiment using phalloidin-FITC conjugate was performed (Kusano et al, 2000). As can be observed in Figure 6, organisation of actin cytoskeleton was completely disturbed by MI-D treatment. Fluorescence labelling of MEL-85 cells treated with MI-D did not give rise to the overall pattern that was observed in control cells, which showed a considerable organisation of F-actin fibres all over the cell body. MI-D treatment induced a reorganisation of the F-actin cytoskeleton architecture. Cells in the presence of MI-D did not spread and the filamentous structures disassembled or were reorganised to accumulate in the submembraneous area. Actin filaments turned into actin granules mainly localised on the edge of MEL-85 cells. These results point to a disruption of interactions between cells and the extracellular matrix.

Figure 6.

Figure 6

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Effects of MI-D on F-actin cytoskeleton organisation of MEL-85 cells. (A) Micrographs of MEL-85 control cells (× 600). (B) MEL-85 control cells at a higher magnification showing details of well-organised F-actin cytoskeleton (× 1450). (C) Micrographs of MEL-85 cells treated with 50 μM MI-D (× 600). (D) MEL-85 treated with 50 μM MI-D, cells under a higher magnification, depicting disturbances to the organisation of F-actin molecules, concentrated at the edge of cells with a granular pattern (arrow) (× 1200). MEL-85 cells were treated with MI-D, fixed and labelled with a phalloidin-FITC conjugate and observed at a confocal fluorescence microscope (Confocal Radiance 2100, Bio-Rad) coupled to a Nikon Eclipse 800 with plan apochromatic objectives.

DISCUSSION

We are now able to show that MI-D has considerable cytotoxic and antiproliferative effects on human melanoma cell lines. These effects seem to be even more aggressive on human melanoma cells than those observed with B16-F10 murine melanoma cells (Senff-Ribeiro et al, 2003, 2004). For example, a dose of 10 μM after 48 h incubation, on B16-F10 melanoma cells diminished their viability to ∼80% (Senff-Ribeiro et al, 2003, 2004) and in all the four human melanoma cell lines the viability was lower than 30% under these conditions. Interestingly, MI-D at a low concentration (5 μM), gave rise to effects of a different magnitude on the viabilities of human melanoma cells. Under this condition, MEL-85 and MEWO cell lines (Figure 2A and D) were more sensitive to MI-D than SK-MEL and A2058 (Figure 2B and C). Inhibitions of different magnitude on the cell growth of different human melanoma cell lines were also observed. The concentration of 5 μM allowed MEL-85 growth at a lower rate than that of the control (Figure 3A), but completely inhibited the growth of SK-MEL cells (Figure 3B). The results on viability and proliferation are compatible. As one can observe in Figures 2 and 3, MI-D was very cytotoxic to human melanoma cells and had also an antiproliferative effect. The antiproliferative effect of MI-D was present at both noncytotoxic and cytotoxic doses. The effects of MI-D on the viability and proliferation of the various human melanoma cell lines show MI-D to be a toxic drug for human melanoma cells.

Since tumour cell adhesion to ECM constituents is a fundamental step in tumour development and invasion (Mishima et al, 1998), we investigated the effect of MI-D on MEL-85 melanoma cells adhesion to laminin, fibronectin and matrigel. Low MI-D doses were used in order to minimise its extensive metabolic effects, so that the drug was used at subcytotoxic concentration to evaluate MEL-85 adhesion to ECM. Overall, 5 μM MI-D caused a slight decrease of ∼5% on MEL-85 viability after 2 h. Under such an experimental condition, MI-D was able to inhibit cell adhesion when it was incubated with the cells for 2 h. Analysing the images of experiments (Figure 4D), we can observe that MI-D treatment promoted loss of cell spreading, which became round, suggesting a possible activity of MI-D on cytoskeleton organisation. These observations were confirmed by morphological and F-actin analyses. Loss of overall cell shape accompanied by cell shrinkage, membrane blebbing and chromatin condensation, besides disturbance of the cytoskeleton organisation, are often observed on apoptotic cells (Hengartner, 2000). The effects of MI-D on MEL-85 adhesion on ECM and morphology may be related to its cytotoxic activity. Although the four different cell lines showed slightly different sensitivities to MI-D, all of them responded to MI-D in a very similar way, so that the MEL-85 results on adhesion, morphology and cytoskeleton organisation probably represent an action of MI-D on human melanoma cell lines.

MI-D is an uncoupler of mitochondrial phosphorylation (Cadena et al, 1998), whose effects on membranes have been recognised (Cadena et al, 2002). Touching on this question, MI-D is an inhibitory uncoupler (Cadena et al, 1998) and according to Skulachev (1998) and others (Colombo et al, 2001), in some instances, an uncoupling action could explain the therapeutic effect of a drug. This seems true for the antitumour action of carbonylcyanide-m-chlorophenylhydrazone (CCCP) (Newell and Tannock, 1989) and other anticancer drugs (Keller et al, 1992). The induction of apoptosis could be a consequence of the cytotoxic activity of MI-D, as it is already known that drugs, which affect mitochondrial metabolism, might facilitate the induction of cell death and overcome apoptosis resistance in cancer cells (Susin et al, 1998; Colombo et al, 2001). Moreover, since membrane proteins are highly dependent on membrane organisation and fluidity (Lopez and Kosk-Kosika, 1997), the effects of MI-D on membranes could disturb recognition sites, which are necessary for adhesion.

In conclusion, MI-D is a potent drug against human melanoma cells and this is the first study on its effects against these cells, as well as for a mesoionic compound of the 1,3,4-thiadiazolium class. Besides its cytotoxic properties, MI-D also interferes in cell features involved in tumour development, such as adhesion to ECM components. These results, combined with previous data (Senff-Ribeiro et al, 2003, 2004) that showed MI-D to be a potent drug against B16-F10 murine melanoma both in vitro and in vivo, emphasise that MI-D could be a promising drug for the treatment and study of melanoma.

Acknowledgments

We thank Professor Dr RR Brentani, Ludwig Institute for Cancer Research (São Paulo, SP, Brazil), for providing the human melanoma cell lines used in our study.

This study was supported by PRONEX, CAPES, FUNDAÇÃO ARAUCÁRIA and CNPq.

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